Canonical Allele Identifier: CA2838523865
Gene: SLC35C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45806341G>T , CM000673.2:g.45806341G>T GRCh38
NC_000011.9:g.45827892G>T , CM000673.1:g.45827892G>T GRCh37
NC_000011.8:g.45784468G>T NCBI36
NG_009875.1:g.7270G>T , LRG_107:g.7270G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.496+5G>T ENSP00000432145.2:n.496+5G>T
ENST00000314134.4:c.535+5G>T MANE Select ENSP00000313318.3:n.535+5G>T
ENST00000314134.3:c.535+5G>T ENSP00000313318.3:n.535+5G>T
ENST00000442528.2:c.496+5G>T ENSP00000412408.2:n.496+5G>T
NM_001145265.1:c.496+5G>T NP_001138737.1:n.496+5G>T
NM_001145266.1:c.496+5G>T NP_001138738.1:n.496+5G>T
NM_018389.4:c.535+5G>T , LRG_107t1:c.535+5G>T NP_060859.4:n.535+5G>T
XM_011520203.1:c.535+5G>T XP_011518505.1:n.535+5G>T
XM_011520203.3:c.535+5G>T XP_011518505.1:n.535+5G>T
NM_001145265.2:c.496+5G>T NP_001138737.1:n.496+5G>T
NM_018389.5:c.535+5G>T MANE Select NP_060859.4:n.535+5G>T